A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460999



Internal ID22518882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2591118..2592417hg38UCSC Ensembl
chr11:2612348..2613647hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864773
Supporting Variants
Samples
Known GenesKCNQ1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460999
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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